Proof of principle of a purine D–A–D′ ligand based ratiometric chemical sensor harnessing complexation induced intermolecular PET. Issue 45 (13th November 2020)

• Record Type: Journal Article
• Authors: Jovaisaite, Justina; Cīrule, Dace; Jeminejs, Andris; Novosjolova, Irina; Turks, Māris; Baronas, Paulius; Komskis, Regimantas; Tumkevicius, Sigitas; Jonusauskas, Gediminas; Jursenas, Saulius
• Is Part Of: Physical chemistry chemical physics. Volume 22:Issue 45(2020)
• Page Start: 26502
• Page End: 26508
• Publication Date: 2020-11-13
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/d0cp04091f
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : A ratiometric fluorescence cation sensor based on an asymmetrically functionalized donor–acceptor–donor′ purine derivative is presented. Abstract : A comprehensive photophysical study of a series of purines, doubly decorated at C2 and C6 positions with identical fragments ranging from electron acceptor to donor groups of different strengths, is presented. The asymmetry of substitutions creates a unique molecular D–A–D′ structure possessing two independent electronic charge transfer (CT) systems attributed to each fragment and exhibiting dual-band fluorescence. Moreover, the inherent property of coordination of metal ions by purines was enriched due to a presence of nearby triazoles used as spacers for donor or acceptor fragments. New molecules present a bidentate coordination mode, which makes the assembly of several ligands with one metal cation possible. This property was exploited to create a new concept of a ratiometric chemical fluorescence sensor involving the photoinduced electron transfer between branches of different ligands as a mechanism of fluorescence modulation.